The discovery and development of P2 receptor subtypes

Charles Kennedy
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引用次数: 26

Abstract

Extracellular purine and pyrimidine nucleotides modulate cellular activity by acting at P2 receptors. The first receptor to be identified was the P2-purinoceptor, which was characterised and named in 1978. In the 1980s this site was subdivided into P2X and P2Y purinoceptors on the basis of pharmacological criteria in functional studies on native receptors. Subsequently, a similar approach led to the characterisation of the P2T, P2Z, P2U and P2D purinoceptors. In the 1990s a molecular biological approach has led to the cloning and functional expression of at least 12 mammalian P2 receptor subtypes. The challenge now is to relate these recombinant receptors to native receptors present within a wide range of tissues.

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P2受体亚型的发现和发展
胞外嘌呤和嘧啶核苷酸通过作用于P2受体调节细胞活性。第一个被鉴定的受体是p2 -嘌呤受体,它在1978年被鉴定并命名。在20世纪80年代,根据天然受体功能研究的药理学标准,该部位被细分为P2X和P2Y嘌呤受体。随后,类似的方法导致了P2T, P2Z, P2U和P2D嘌呤受体的表征。在20世纪90年代,一种分子生物学方法导致了至少12种哺乳动物P2受体亚型的克隆和功能表达。现在的挑战是将这些重组受体与存在于广泛组织中的天然受体联系起来。
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